About: Spinal Muscular Atrophy

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Spinal Muscular Atrophy
rdfs:subClassOf	Muscular Diseases Rare Non-Neoplastic Disorder
Has_NICHD_Parent	Nervous System Malformations
Concept_In_Subset	NICHD Terminology Neonatal Research Network Terminology
Semantic_Type	Disease or Syndrome
Preferred_Name	Spinal Muscular Atrophy
UMLS_CUI	C0026847
Contributing_Source	NICHD
FULL_SYN	Spinal Muscular AtrophyPTNCI Spinal Muscular AtrophyPTNICHD
DEFINITION	An inherited disorder characterized by degeneration of the spinal cord and the cerebellum. Symptoms may appear at any age and include progressive loss of coordination of gait, hands, speech, and eye movements.NCI
code	C85075
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0014250
is rdfs:subClassOf of	Werdnig-Hoffmann Disease Spinal Muscular Atrophies of Childhood
is Has_NICHD_Parent of	Werdnig-Hoffmann Disease
is sameAs of	Muscular Atrophy, Spinal

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